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Characterizing the Association Between Preoperative Depressive Symptoms and Opioid Use/Misuse After Surgery

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Stanford University

Status

Completed

Conditions

Opioid Use

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

This observational study aims to characterize the relationship between preoperative depressive symptoms and opioid use/ misuse after surgery using a perioperative learning health care system. We will follow a prospective cohort of patients undergoing elective surgery.

Enrollment

718 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Age 18+
  2. Planning to undergo surgery
  3. English speaking
  4. Ability and willingness to complete questionnaires and assessments

Exclusion criteria

  1. Any conditions causing inability to complete assessments (education, cognitive ability, mental status, medical status)
  2. Known Pregnancy
  3. Elevated Suicidality
  4. Enrollment in a conflicting perioperative trial

Trial design

718 participants in 1 patient group

Patients undergoing elective operations
Description:
We will follow a prospective cohort of 558 patients, undergoing any elective surgery at Stanford Hospital. Subjects will undergo baseline and longitudinal testing via a (including NIH Patient-Reported Outcomes Measurement Information System- PROMIS measures of emotional distress). After surgery, participants will report weekly changes in opioid use, pain, and adverse events; and monthly changes in opioid misuse for 1 year.

Trial documents
1

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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